Siblings of neonatal hyperbilirubinemia with UGT1A1 double missense variants.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 195, doi. 10.1297/cpe.2024-0028
- By:
- Publication type:
- Article
Works matching IS 09185739 AND DT 2024 AND VI 33 AND IP 3
Results: 14
1
2
Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 187, doi. 10.1297/cpe.2024-0004
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- Publication type:
- Article
3
Severe growth retardation during carbohydrate restriction in type 1 diabetes mellitus: A case report.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 181, doi. 10.1297/cpe.2024-0003
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- Publication type:
- Article
4
A case of diffuse congenital hyperinsulinism in which continuous glucose monitoring contributed to the choice of a treatment strategy following a subtotal pancreatectomy.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 174, doi. 10.1297/cpe.2023-0086
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- Publication type:
- Article
5
PTPN11 and FLNA variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 169, doi. 10.1297/cpe.2023-0074
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- Publication type:
- Article
6
Adipsic hypernatremia with marked hyperprolactinemia and GH deficiency in a 9-year-old boy.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 163, doi. 10.1297/cpe.2024-0001
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- Publication type:
- Article
7
Potential indication of chemotherapy for hypodipsia and arginine vasopressin deficiency secondary to hypothalamic-pituitary Langerhans cell histiocytosis: a case report and literature review.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 157, doi. 10.1297/cpe.2024-0002
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- Publication type:
- Article
8
Pseudohypoparathyroidism type 1B with involuntary movements: a case report and literature review.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 151, doi. 10.1297/cpe.2023-0080
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- Publication type:
- Article
9
A case of long-term survival of SADDAN treated with growth hormone for marked short stature.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 144, doi. 10.1297/cpe.2023-0068
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- Publication type:
- Article
10
Traumatic brain injury inducing swift transition from syndrome of inappropriate antidiuretic hormone secretion to central diabetes insipidus: a case report.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 139, doi. 10.1297/cpe.2023-0057
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- Publication type:
- Article
11
Use of a long-term continuous glucose monitor for predicting sulfonylurea dose in patients with neonatal diabetes mellitus: a case series.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 131, doi. 10.1297/cpe.2023-0062
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- Publication type:
- Article
12
Peak expiratory flow, core performance and physical activity in normal-weight, overweight, and obese adolescents.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 124, doi. 10.1297/cpe.2024-0019
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- Publication type:
- Article
13
Clinical characteristics in children with maturity-onset diabetes of the young detected by urine glucose screening at schools in the Tokyo Metropolitan Area.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 113, doi. 10.1297/cpe.2024-0009
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- Publication type:
- Article
14
Delayed menarche in children and adolescents with type 1 diabetes mellitus: a systematic review and meta-analysis.
- Published in:
- Clinical Pediatric Endocrinology, 2024, v. 33, n. 3, p. 104, doi. 10.1297/cpe.2023-0058
- By:
- Publication type:
- Article